Spinal Plate And Locking Screw Devices, Methods, And Systems

ABSTRACT

An embodiment of the invention provides for a system, such as a cervical plate fusion system, that has mechanisms for preventing bone screws from backing out of the plate. The system prevents both counter-rotation of the screw and axial backing out of the screw. Other embodiments are described herein.

BACKGROUND

Spinal fixation devices can be used to provide, for example,immobilization and stabilization of spinal segments in patients (e.g.,humans, dogs, cats, and other animals). Fixation devices may be used tohelp fuse bone segments (e.g., vertebrae) in the treatment ofinstabilities or deformities of, for example, the cervical, thoracic,lumbar, and/or sacral spine. Such instabilities or deformities mayinclude, for example, degenerative disc disease (DDD);spondylolisthesis; trauma (i.e., fracture or dislocation); spinalstenosis; curvatures (i.e., scoliosis, kyphosis, and/or lordosis);tumor; pseudoarthrosis; and failed previous fusions.

However, there are risks associated with such fixation devices. Suchrisks include, for example, device component fracture, loss of fixationwhen the device/tissue bond is weakened or lost, non-union, fracture ofthe vertebra, neurological injury, and vascular or visceral injury. Forexample, internal fixation appliances are load sharing devices used toobtain bone alignment until normal healing occurs. Thus, implants aresubjected to loads such as repetitive loads that occur when fixationsystems are subjected to loading associated with, for example, normalpatient movements (e.g., walking and bending), delayed union, ornon-union situations. These loads can cause screws, which couple afixation plate to bone, to loosen. The screws may loosen by, forexample, backing out. This “backing out” may occur due to unwanted screwrotation (e.g., when the screw rotates and “unscrews” from the bone)and/or unwanted screw axial movement that is directed away from thebone. The axial movement may or may not be caused by the unwanted screwrotation. When a screw or screws back out and away from the plate andbone, the plate may become unstable and lead to complications for thepatient. The degree or success of union, loads produced by weightbearing, and activity levels will, among other conditions, dictate thelongevity of the implant. Robust fixation systems are needed to lessenrisks associated with fixation and to promote better outcomes forpatients.

BRIEF DESCRIPTION OF THE DRAWINGS

Features and advantages of embodiments of the present invention willbecome apparent from the appended claims, the following detaileddescription of one or more example embodiments, and the correspondingfigures, in which:

FIGS. 1 a-c include different perspectives of a plate in an embodimentof the invention.

FIGS. 2 a-c include different perspectives of a resilient member in anembodiment of the invention.

FIGS. 3 a-e include different perspectives of a screw in an embodimentof the invention.

FIGS. 4 a-e include different perspectives of a plate in an embodimentof the invention.

FIG. 5 includes a schematic flow chart for a method in an embodiment ofthe invention.

FIG. 6 includes various implant states for an embodiment of theinvention.

DETAILED DESCRIPTION

In the following description, numerous specific details are set forth.However, it is understood that embodiments of the invention may bepracticed without these specific details. Well-known structures andtechniques have not been shown in detail to avoid obscuring anunderstanding of this description. References to “one embodiment”, “anembodiment”, “example embodiment”, “various embodiments” and the likeindicate the embodiment(s) so described may include particular features,structures, or characteristics, but not every embodiment necessarilyincludes the particular features, structures, or characteristics.Further, some embodiments may have some, all, or none of the featuresdescribed for other embodiments. Also, as used herein “first”, “second”,“third” and the like describe a common object and indicate thatdifferent instances of like objects are being referred to. Suchadjectives are not intended to imply the objects so described must be ina given sequence, either temporally, spatially, in ranking, or in anyother manner. Also, the terms “coupled” and “connected,” along withtheir derivatives, may be used. In particular embodiments, “connected”may be used to indicate that two or more elements are in direct physicalcontact with each other and “coupled” may mean that two or more elementsco-operate or interact with each other, but they may or may not be indirect physical contact.

An embodiment of the invention provides for a system, such as a cervicalplate fusion system, that has mechanisms for preventing bone anchors(e.g., screws, pins, and the like) from backing out of the plate. Thesystem prevents both counter-rotation of the screw and axial backing outof the screw. Other embodiments are described herein.

FIGS. 1 a-c include plate 100. Plate 100 may be used for fusion ofcervical vertebrae but may also be used for fusion of other vertebrae(e.g., thoracic, lumbar) or for fixation of other tissues (e.g.,adjacent bone sections of a femur or other bone or tissue) and the like.

Plate 100 includes apertures 101, 102, 103, 104, 105, 106. Theseapertures or holes may have continuous perimeters but may also includediscontinuous perimeters that do not form a complete circle, oval,rectangle and the like. The apertures (e.g., holes) need not becircular, symmetrical, or have any one particular perimeter, even thoughapertures 101, 102, 103, 104, 105, 106 each include a generallycontinuous circular perimeter. The three pairs of holes (101 and 104,102 and 105, 103 and 106) of plate 100 are for a two level fusion systemwhere two vertebral discs are to be fused. For example, only holes 101,102, 104, 105 would be needed for a one level fusion. (FIG. 4 a isconfigured for a one level fusion system.) A fourth pair of holes may beneeded for a three level fusion.

Plate 100 includes cavities 115, 116, 117. Cavity 115 is described ingreater detail herein but functions largely in the same manner ascavities 116, 117. Cavity 115 connects to holes 101, 104.

As seen in FIGS. 1 a-c, single-piece monolithic resilient members 118,119, 120 are respectively included in cavities 115, 116, 117. Resilientmember 118 is described in greater detail herein but functions largelyin the same manner as resilient members 119, 120. In FIGS. 2 a-c, member218 includes arms 252, 258 respectively connected to ends having fins209, 212. During manufacturing member 218 may be stamped out in the “S”pattern shown in FIGS. 2 a-b. The stamped member may be stamped out as asingle monolithic element with no weldings or fixtures used to assemblemember 218.

In FIGS. 3 a-e, screw 340 includes lip 341, which is coupled to anangled or beveled shoulder 344, and a toothed wheel 365 having teethsuch as tooth 348 and tooth 349.

FIG. 5 includes method 500, which addresses various embodiments of theinvention. For example, in block 505 a user inserts screw 340 into hole101 of plate 100. Cavity 115 includes channels 121, 151 thatrespectively include first and second portions of resilient member 118.Fins 109, 112 respectively project into holes 101, 104. Thus, at least aportion of fins 109, 112 project into holes 101, 104.

In an embodiment, resilient member 118 is seperably coupled to plate100. For example, during assembly (e.g., at a manufacturing plant, in anoperating room, in a medical office, etc.) member 118 may be compressedand then inserted into cavity 115. In an embodiment, member 118 isretained within cavity 115 based on a resistance fit where member 118does not require use of a weld, screw, clamp, or the like to hold member118 within cavity 115. Consequently, member 118 has advantages relatedto ease of manufacturing and also related to ease of assembly into plate100. In an embodiment, cavity 118 remains generally open and un-enclosedupon final implantation of the system into the patient. Also, placingmember 118 within (partially or fully) cavity 115 helps reduce theoverall profile of the plate system, thus providing a less intrusivesystem for the patient.

As seen in FIG. 2, fin 209 has an angled leading edge 223 and a curvedtrailing edge 224, leading edge 223 being non-orthogonally connected toarm 252. Regarding the screw that interfaces member 218, FIG. 3 showshow tooth 348 has angled leading edge 342 and curved trailing edge 343,leading edge 342 being non-orthogonal to tangent 354 that intersectstoothed wheel 365 at the same point as angled leading edge 342. Fin 209is sized to be received between teeth 348, 349 of toothed wheel 365.

In FIG. 6, state 605 depicts an embodiment of the invention with a screwinserted into a hole.

Returning to FIG. 5, in block 510 shoulder 344 of screw 340 deflectsmember 118. Specifically, when screw 340 is in a partially implantedposition and is being inserted into hole 101 beveled shoulder 344 isactively deflecting fin 109 medially towards cavity 115. In FIG. 6,state 610 depicts an embodiment of the invention with a fin deflected bya shoulder.

In block 515, the user advances screw 340 into a fully implantedposition such that screw 340 is prevented from backing out of hole 101by fin 109. In block 520 fin 109 has snapped back laterally (afterhaving been deflected medially in block 510) into hole 101 to nowintercept lip 341 if and when screw 340 “backs out” or travels (orattempts to “back out” or travel) axially away from patient bone inwhich it is implanted. Also, while toothed wheel 365 is allowed torotate in one direction (e.g., clockwise to tighten screw 340 into bone)toothed wheel 365 is prevented from counter-rotating (e.g., counterclockwise to loosen and “back out” from bone) because trailing edge 224of fin 209 is lodged against trailing edge 343 of tooth 348. In FIG. 6,items 615, 620 depicts an embodiment of the invention with a fin“snapped back laterally.”

FIG. 4 includes an embodiment of the invention where holes 401, 404 arebisected by horizontal axis 455, which is orthogonal to the midline of apatient in which the system is configured for implantation and long axis456 of plate 400. Plate 400 also includes holes 402, 405 and anothercavity (e.g., cavity 116). Holes 402, 405 are bisected by horizontalaxis 457, which is orthogonal to long axis 456. Plate 400 includesviewing aperture 407, which allows patient tissue to be viewed by a userupon implantation of the system into a patient, located along long axis456 and fully or partially between axes 455, 457. Bone tissue may beinserted through aperture 407 to facilitate fusion. As seen in FIG. 1,member 118 does not project into aperture 107. Also, cavity 115 does notconnect to aperture 107. Returning to FIG. 4, 401, 402, 404, 405 are allincluded in a single level of the plate, the single level correspondingto a single level of fusion within the patient.

In an embodiment, member 118 includes nitonol. However, in otherembodiments member 118 includes other materials such as stainless steeland the like. In an embodiment, member 118 includes an “S” shapedprofile but may include other shaped profiles (e.g., ovular, circular)in other embodiments. In an embodiment, arm 252 couples to arm 258 viabody 253. When resilient member 218 is fully compressed for insertioninto cavity 115 arms 252, 258 may both be compressed against body 253.

In an embodiment, screw 340 includes tooth 348, which has a height 359sized so when the screw is fully implanted (e.g., with shoulder 344directly against bone) fin 109 will always be in contact with a portionof tooth 348. In other words, in an embodiment fin 109 projects mediallyout from “T” channel 421 (FIG. 4). If height 359 is too small, fin 109could spring or project over tooth 348 and possibly loose contact withtooth 348. In such a case screw 340 may begin working loose when not inconstant contact with a tooth include on the toothed wheel because therewould be no immediate barrier to axial “back out” movement and/orloosening counter-rotation. However, such a scenario may be mitigated oreliminated by properly sizing height 359 so when the screw is fullyimplanted fin 109 will always be in contact with a portion of tooth 348.

In an embodiment, horizontal axis 461 intercepts the first and secondfins (not shown) of a single level. Axis 461 does not intercept lateralwall portion 462 of hole 401 but does intercept medial wall 463 of hole401. Thus curvature of the plate provides for proper lordosis. Also,having horizontal axis 461 intercept the first and second fins of asingle level provides benefits in manufacturing as plates with one, two,or three fusion levels are of similar design but for using one, two, orthree resilient members. Thus, the design of the system allows forscaling between various embodiments that correspond to varying fusionlevels.

In various embodiments, resilient member 218 includes dimension 230 ofgenerally 0.3, 0.4, 0.5, 0.6, 0.7, or 0.8 mm. Member 218 includesdimension 233 of generally 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, or 1.8 mm.Member 218 includes dimension 225 of generally 6.5, 6.6, 6.7, 6.8, 6.9,7.0, 7.1, 7.2, 7.3, or 7.4 mm. Member 218 includes dimension 232 ofgenerally 0.3, 0.4, 0.5, 0.6, or 0.7 mm. Member 218 includes dimension234 of generally 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 mm. Member 218includes dimension 229 of generally 0.1, 0.2, 0.3, 0.4, or 0.5 mm.Member 218 includes dimension 228 of generally 0.3, 0.4, 0.5, 0.6, 0.7,0.8, or 0.9 mm. Member 218 includes dimension 226 of generally 0.4, 0.5,0.6, 0.7, 0.8, 0.9, or 1.0 mm. Member 218 includes dimension 227 ofgenerally 0.1, 0.2, 0.3, 0.4, 0.5, or 0.6 mm. However, other sizings anddimensions are within the scope of the embodiments and may be dictatedaccording to load requirements (e.g., amount of load, duration of loadbearing, etc.).

In various embodiments screw 340 includes height 359 of generally 1.2,1.3, 1.4, 1.5, 1.6, 1.7, or 1.8 mm. Screw 340 includes dimension 360 ofgenerally 2.8, 2.9, 3.0, 3.1, 3.2, or 3.3 mm. Screw 340 includesdimension 345 of generally 0.1, 0.2, 0.3, 0.4, 0.5, or 0.6 mm. Screw 340includes dimension 346 of generally 60, 65, 70, 75, 80, or 85 degrees.Screw 340 includes dimension 347 of generally 0.1, 0.2, 0.3, or 0.4 mm.

In various embodiments plate 400 includes dimension 450 of generally0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1.0 mm.

In one embodiment, a medial force directed to fin 109 translates to alateral force directed to fin 112. Thus, a counter-rotation of a screwin hole 101 may produce a medial force against fin 109, which may thentranslate along monolithic member 118 and into a lateral force along fin112, which may prevent a screw in hole 104 from counter-rotating or evenmoving axially and backing out.

In various embodiments, a plate may forego use of a cavity (thatcorresponds to a resilient member) and may instead couple the resilientmember to an outer surface of the plate. The resilient member may alsobe integral or monolithic with the plate. Also, fins may include variousgeometries and may include, for example, orthogonal dimensions such thatthe fin has straight edges that fit at right angles to an arm ofresilient member. The fin may be rectangular, square, and the like. Thesame may be the case for teeth on the screw such that the teeth may havestraight edges that fit at right angles to the toothed wheel. Resilientmembers do not necessarily need to project into two holes. Instead, forexample, a resilient member may be dedicated to a single hole andresisting backing out of the single screw that corresponds to the singlehole. Also, a single resilient member may be applied to three or moreholes. In such a case, the broader resilient member may be included inor over a cavity that, for example, winds around the plate with channelsconnecting to three or more holes. Also, embodiments do not necessarilyrequire that the screw include a “highly” toothed wheel but may alsoinclude a screw with a few (e.g., one or two) simple projections thatserve as teeth to accomplish the goal of preventing unwanted rotation.Also, while “rotation” and “counter rotation” have been used hereinthose terms should not be assumed to be associated with, for example,any particular direction such as “clockwise” for “rotation” or “counterclockwise” for “counter rotation.” Also, screws may include lips thatare not necessarily limited to flanges and the like. Lips may includefloors or basic impediments to, for example, vertical or axial movementaway from bone.

While the present invention has been described with respect to a limitednumber of embodiments, those skilled in the art will appreciate numerousmodifications and variations therefrom. It is intended that the appendedclaims cover all such modifications and variations as fall within thetrue spirit and scope of this present invention.

What is claimed is:
 1. An orthopedic fusion system comprising: a platethat includes first and second holes and a first cavity connecting thefirst and second holes; a single-piece monolithic resilient memberincluded in the first cavity, the resilient member including a first armconnected to a first end having a first fin and a second arm connectedto a second end having a second fin; a screw including a lip, which iscoupled to a beveled shoulder, and a toothed wheel having first andsecond teeth; wherein (a) the resilient member is seperably coupled tothe plate and within the first cavity; (b) the first cavity includesfirst and second channels that respectively include first and secondportions of the resilient member; (c) the first and second finsrespectively project into the first and second holes; (d) the first finhas a first angled leading edge and a first curved trailing edge, thefirst angled leading edge of the first fin being non-orthogonallyconnected to the first arm; (e) the first tooth has a first angledleading edge and a first curved trailing edge, the first angled leadingedge of the first tooth being non-orthogonal to a tangent intersectingthe toothed wheel at a same point the first angled leading edge of thefirst tooth intersects the toothed wheel; and (f) the first fin is sizedto be received between the first and second teeth of the toothed wheel;wherein the system is configured such that (g) in a partially implantedposition the screw is inserted into the first hole and the beveledshoulder is actively deflecting the first fin medially towards the firstcavity; and (h) in a fully implanted position (1) the screw is insertedinto the first hole such that the screw is prevented from backing out ofthe first hole by the first fin that has snapped back into the firsthole to intercept the lip when the screws travels axially away frompatient bone in which it is implanted and (2) the toothed wheel isallowed to rotate but is prevented from counter-rotating because thefirst curved trailing edge of the first fin is lodged against the firsttrailing edge of the first tooth.
 2. The system of claim 1, wherein theresilient member includes nitonol.
 3. The system of claim 1, wherein thefirst and second holes are bisected by a first horizontal axis, which isorthogonal to the (a) midline of a patient in which the system isconfigured for implantation and (b) a long axis of the plate.
 4. Thesystem of claim 3, wherein: the plate includes third and fourth holesand a second cavity connecting the third and fourth holes, the third andfourth holes being bisected by a second horizontal axis that isorthogonal to the midline of the patient and the long axis of the plate;a first viewing aperture, which allows patient tissue to be viewed uponimplantation of the system, located along the long axis of the plate andbetween the first and second horizontal axes; the first resilient memberdoes not project into the first viewing aperture; the first cavity doesnot connect to the first view aperture; and the first, second, third,and fourth holes are all included in a single level of the plate, thesingle level corresponding to a level of fusion within the patient. 5.The system of claim 3, wherein: the plate includes third and fourthholes and a second cavity connecting the third and fourth holes, thethird and fourth holes being bisected by a second horizontal axis thatis orthogonal to the midline of the patient and the long axis of theplate; a first viewing aperture, which allows patient tissue to beviewed upon implantation of the system, located along the long axis ofthe plate and between the first and second horizontal axes; the firstresilient member does not project below any portion of the first viewingaperture; the first cavity does not project below any portion of thefirst viewing aperture; the first cavity does not connect to the firstview aperture; the first, second, third, and fourth holes each include acontinuous enclosed perimeter separate and apart from a perimeter of theviewing aperture; and the first, second, third, and fourth holes are allincluded in a single level of the plate, the single level correspondingto a level of fusion within the patient.
 6. The system of claim 1,wherein the first resilient member is retained within the first cavitybased on a resistance fit and without use of a weld, screw, or clamp. 7.The system of claim 1, wherein the first resilient member includes an“S” shaped profile.
 8. The system of claim 1, wherein the first toothincludes a first height, as measured from the lip to the top of thefirst tooth, which is sized so when the screw is fully implanted thefirst fin will always be in contact with a portion of the first tooth.9. The system of claim 1, wherein the first arm connects to the secondarm via a first body so when the resilient member is fully compressedfor insertion into the first cavity the first and second arms may bothbe compressed against the first body.
 10. The system of claim 1, whereinthe first cavity remains open and un-enclosed upon final implantation ofthe system into the patient.
 11. The system of claim 1, wherein ahorizontal axis (a) intercepts the first and second fins, (b) does notintercept a lateral wall of the first hole, and (c) intercepts a medialwall of the first hole.
 12. An orthopedic system comprising: a platethat includes first and second holes; a resilient member including afirst arm and a second arm; a bone anchor including a lip, which iscoupled to a shoulder, and first and second teeth; wherein (a) the firstand second arms respectively project to the first and second holes; (b)the first arm has a first leading edge and a first trailing edge; (c)the first tooth has a first leading edge and a first trailing edge; and(d) the first arm is sized to be received between the first and secondteeth; wherein the system is configured such that (e) in a partiallyimplanted position the bone anchor is inserted into the first hole andthe shoulder is actively deflecting the first arm; and (f) in a fullyimplanted position (1) the bone anchor is inserted into the first holesuch that the bone anchor is prevented from backing out of the firsthole by the first arm that has snapped back to the first hole tointercept the lip when the bone anchor travels axially away from patientbone in which it is implanted, and (2) the bone anchor is allowed torotate but is prevented from counter-rotating because the first trailingedge of the first arm is lodged against the first trailing edge of thefirst tooth.
 13. The system of claim 12, wherein the first and secondholes are bisected by a first horizontal axis, which is orthogonal tothe (a) midline of a patient in which the system is configured forimplantation and (b) a long axis of the plate.
 14. The system of claim12, wherein the first tooth includes a first height, as measured fromthe lip to the top of the first tooth, which is sized so when the boneanchor is fully implanted the first end will always be in contact with aportion of the first tooth.
 15. The system of claim 12, wherein ahorizontal axis (a) intercepts the first and second arms, (b) does notintercept a lateral wall of the first hole, and (c) intercepts a medialwall of the first hole.
 16. An orthopedic system comprising: a platethat includes first and second holes and a first cavity connecting thefirst and second holes; a single-piece monolithic resilient memberconfigured to be included in the first cavity, the resilient memberincluding a first arm connected to a first end having a first fin and asecond arm connected to a second end having a second fin; wherein (a)the resilient member is seperably coupled to the plate and within thefirst cavity; (b) the first cavity includes first and second channelsthat respectively include first and second portions of the resilientmember; (c) the first and second fins respectively project into thefirst and second holes; (d) the first fin has a first angled leadingedge and a first curved trailing edge, the first angled leading edge ofthe first fin being non-orthogonally connected to the first arm; (e) thefirst fin is sized to be received between the first and second teeth ofthe toothed wheel; wherein the system is configured such that (f) when abone anchor, in a partially implanted position, is inserted into thefirst hole a beveled shoulder included in the bone anchor activelydeflects the first fin medially towards the first cavity; and (h) whenthe bone anchor, in a fully implanted position, is inserted into thefirst hole (1) the bone anchor is prevented from backing out of thefirst hole by the first fin that has snapped back into the first hole tointercept a lip, included in the bone anchor, when the bone anchortravels axially away from patient bone in which it is implanted, and (2)the bone anchor is allowed to rotate but is prevented fromcounter-rotating because the first curved trailing edge of the first finis lodged against a first trailing edge of a first tooth included in thebone anchor.
 17. The system of claim 16, wherein the first and secondholes are bisected by a first horizontal axis, which is orthogonal tothe (a) midline of a patient in which the system is configured forimplantation and (b) a long axis of the plate.
 18. The system of claim16, wherein the first tooth includes a first height, as measured fromthe lip to the top of the first tooth, which is sized so when the boneanchor is fully implanted the first fin will always be in contact with aportion of the first tooth.
 19. The system of claim 18, wherein ahorizontal axis bisects the first and second fins and the horizontalaxis does not intercept a lateral wall of the first hole but doesintercept a medial wall of the first hole.
 20. The system of claim 1,wherein the resilient member is configured so a medial force directed tothe first fin translates to a lateral force directed to the second fin.